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238077000: Polygenic hypercholesterolemia (disorder)


Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
356867016 Polygenic hypercholesterolaemia en Synonym Active Case insensitive SNOMED CT core
356868014 Sporadic hypercholesterolemia en Synonym Active Case insensitive SNOMED CT core
356869018 Sporadic hypercholesterolaemia en Synonym Active Case insensitive SNOMED CT core
356870017 Polygenic hypercholesterolemia en Synonym Active Case insensitive SNOMED CT core
626910017 Polygenic hypercholesterolemia (disorder) en Fully specified name Active Case insensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Polygenic hypercholesterolaemia Has definitional manifestation Serum cholesterol raised false Inferred relationship Some
Polygenic hypercholesterolaemia Occurrence Congenital false Inferred relationship Some
Polygenic hypercholesterolaemia Finding site Body system structure false Inferred relationship Some
Polygenic hypercholesterolaemia Is a Primary hypercholesterolaemia true Inferred relationship Some
Polygenic hypercholesterolaemia Has interpretation Above reference range true Inferred relationship Some 1
Polygenic hypercholesterolaemia Interprets Serum total cholesterol measurement true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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